Study on Cytochrome P450 Family 1 B1 Gene Mutations in Primary Congenital Glaucoma Affected Egyptian Patients

Aims: A leading cause of childhood blindness is primary congenital glaucoma (PCG). In early infancy, primary congenital glaucoma manifests and is characterized by elevated IOP, broad cornea, and Haab striae. Often seen are varying degrees of corneal haze, photophobia, epiphora, and blepharospasm. The most-mutated gene associated with PCG is the cytochrome P450 family 1, subfamily…
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February 8, 2021 0